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Author

Mohammad Ali Faghihi

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Galatea Bio (United States)ORCID 0000-0002-8330-9067Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 1Organism:human· 1Approach:statistical model· 1Assay:whole-exome sequencing· 1Assay:whole-genome sequencing· 1

Frequent Co-Authors

Alexander G. IoannidisiD· 1 sharedAlexandro J. MartagóniD· 1 sharedArturo López PinedaiD· 1 sharedBabak MoatamediD· 1 sharedCarlos D. BustamanteiD· 1 sharedConsuelo D. Quinto-CortésiD· 1 sharedDaniel Elías-LópeziD· 1 sharedDaniel Mas MontserratiD· 1 shared

Activity by Year

2025-2025 · peak 1/yr
012025: 1 paper (click to filter)12025

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links
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FaghihiAlexander G. Ioannidis · 1 shared paperIoannidis · 1Alexandro J. Martagón · 1 shared paperMartagón · 1Arturo López Pineda · 1 shared paperPineda · 1Babak Moatamed · 1 shared paperMoatamed · 1Carlos D. Bustamante · 1 shared paperBustamante · 1Consuelo D. Quinto-Cortés · 1 shared paperQuinto-Cortés · 1Daniel Elías-López · 1 shared paperElías-López · 1Daniel Mas Montserrat · 1 shared paperMontserrat · 1David Bonet · 1 shared paperBonet · 1FH Mexican Registry Group · 1 shared paperGroup · 1
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1 shared paperGenetic & Genomic Medicine
Alexander G. IoannidisORCID

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1 paper

Recent·Most cited

Analysis of a deeply-phenotyped familial hypercholesterolemia cohort from Mexico shows a role for both rare and common alleles across known dyslipidemia genes and reveals structural variation in a novel locus.

Nicholas Katsanis, Niki Mourtzi, Consuelo D. Quinto-Cortés, Alexandro J. Martagón, Alexander G. Ioannidis, Francisco M. De La Vega, Jeff Gulcher, Ming Ta Michael Lee, Mohammad Ali Faghihi, Arturo López Pineda, Sonia Moreno–Grau, Daniel Mas Montserrat, Míriam Barrabés, David Bonet, Pavel Salazar Fernández, , Carlos D. Bustamante

The paper analyzes a Mexican FH cohort to show rare and common alleles in FH genes and a novel locus contribute to disease risk, with replication in UK Biobank.

Human Genomics · Nov 24, 2025Peer-reviewedGenetic & Genomic Medicine